Denosumab and Mortality in a Real-World Setting: A Comparative Study.
- Publisher:
- WILEY
- Publication Type:
- Journal Article
- Citation:
- J Bone Miner Res, 2023, 38, (12), pp. 1757-1770
- Issue Date:
- 2023-12
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jbmr4930.pdf | Published version | 795 kB | Adobe PDF |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Alarkawi, D | |
dc.contributor.author | Tran, T | |
dc.contributor.author | Chen, W | |
dc.contributor.author | March, LM | |
dc.contributor.author | Blyth, FM | |
dc.contributor.author | Blank, RD | |
dc.contributor.author | Bliuc, D | |
dc.contributor.author | Center, JR | |
dc.date.accessioned | 2024-03-20T23:21:19Z | |
dc.date.available | 2023-10-21 | |
dc.date.available | 2024-03-20T23:21:19Z | |
dc.date.issued | 2023-12 | |
dc.identifier.citation | J Bone Miner Res, 2023, 38, (12), pp. 1757-1770 | |
dc.identifier.issn | 0884-0431 | |
dc.identifier.issn | 1523-4681 | |
dc.identifier.uri | http://hdl.handle.net/10453/176959 | |
dc.description.abstract | Denosumab (Dmab) is increasingly prescribed worldwide. Unlike bisphosphonates (BPs), its effect on mortality has yet to be well explored. This study examined the association between Dmab and all-cause mortality compared with no treatment in subjects with a fracture and BPs in subjects without a fracture. The study population was from the Sax Institute's 45 and Up Study (n = 267,357), a prospective population-based cohort with questionnaire data linked to hospital admissions (Admitted Patients Data Collection [APDC] data were linked by the Centre for Health Record Linkage), medication records (Pharmaceutical Benefits Scheme [PBS] provided by Services Australia), and stored securely (secure data access was provided through the Sax Institute's Secure Unified Research Environment [SURE]). The new-user cohort design with propensity-score (PS) matching was implemented. In the fracture cohort, Dmab and oral BP users were matched 1:2 to no treatment (Dmab: 617 women, 154 men; oral BPs: 615 women, 266 men). In the no-fracture cohort, Dmab users were matched 1:1 with oral BPs and zoledronic acid (Zol) users (Dmab:oral BPs: 479 men, 1534 women; Dmab:Zol: 280 men, 625 women). Mortality risk was measured using sex-specific pairwise multivariable Cox models. In the fracture cohort, compared with no treatment, Dmab was associated with 48% lower mortality in women (hazard ratio [HR] = 0.52, 95% confidence interval [CI] 0.36-0.72) but not in men. Oral BPs were associated with 44% lower mortality in both sexes (women HR = 0.56, 95% CI 0.42-0.77; men HR = 0.56, 95% CI 0.40-0.78). In the no-fracture cohort, compared with BPs, Dmab was associated with 1.5- to 2.5-fold higher mortality than oral BPs (women HR = 1.49, 95% CI 1.13-1.98; men HR = 2.74; 95% CI 1.82-4.11) but similar mortality to Zol. Dmab in women and oral BPs were associated with lower post-fracture mortality than no treatment. However, Dmab users had generally higher mortality than oral BP users in those without fractures. © 2023 American Society for Bone and Mineral Research (ASBMR). | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | WILEY | |
dc.relation.ispartof | J Bone Miner Res | |
dc.relation.isbasedon | 10.1002/jbmr.4930 | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 06 Biological Sciences, 09 Engineering, 11 Medical and Health Sciences | |
dc.subject.classification | Anatomy & Morphology | |
dc.subject.classification | 31 Biological sciences | |
dc.subject.classification | 32 Biomedical and clinical sciences | |
dc.subject.mesh | Male | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Female | |
dc.subject.mesh | Bone Density Conservation Agents | |
dc.subject.mesh | Denosumab | |
dc.subject.mesh | Prospective Studies | |
dc.subject.mesh | Diphosphonates | |
dc.subject.mesh | Zoledronic Acid | |
dc.subject.mesh | Fractures, Bone | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Diphosphonates | |
dc.subject.mesh | Prospective Studies | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Bone Density Conservation Agents | |
dc.subject.mesh | Fractures, Bone | |
dc.subject.mesh | Denosumab | |
dc.subject.mesh | Zoledronic Acid | |
dc.subject.mesh | Male | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Female | |
dc.subject.mesh | Bone Density Conservation Agents | |
dc.subject.mesh | Denosumab | |
dc.subject.mesh | Prospective Studies | |
dc.subject.mesh | Diphosphonates | |
dc.subject.mesh | Zoledronic Acid | |
dc.subject.mesh | Fractures, Bone | |
dc.title | Denosumab and Mortality in a Real-World Setting: A Comparative Study. | |
dc.type | Journal Article | |
utslib.citation.volume | 38 | |
utslib.location.activity | United States | |
utslib.for | 06 Biological Sciences | |
utslib.for | 09 Engineering | |
utslib.for | 11 Medical and Health Sciences | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
utslib.copyright.status | closed_access | * |
dc.date.updated | 2024-03-20T23:21:18Z | |
pubs.issue | 12 | |
pubs.publication-status | Published | |
pubs.volume | 38 | |
utslib.citation.issue | 12 |
Abstract:
Denosumab (Dmab) is increasingly prescribed worldwide. Unlike bisphosphonates (BPs), its effect on mortality has yet to be well explored. This study examined the association between Dmab and all-cause mortality compared with no treatment in subjects with a fracture and BPs in subjects without a fracture. The study population was from the Sax Institute's 45 and Up Study (n = 267,357), a prospective population-based cohort with questionnaire data linked to hospital admissions (Admitted Patients Data Collection [APDC] data were linked by the Centre for Health Record Linkage), medication records (Pharmaceutical Benefits Scheme [PBS] provided by Services Australia), and stored securely (secure data access was provided through the Sax Institute's Secure Unified Research Environment [SURE]). The new-user cohort design with propensity-score (PS) matching was implemented. In the fracture cohort, Dmab and oral BP users were matched 1:2 to no treatment (Dmab: 617 women, 154 men; oral BPs: 615 women, 266 men). In the no-fracture cohort, Dmab users were matched 1:1 with oral BPs and zoledronic acid (Zol) users (Dmab:oral BPs: 479 men, 1534 women; Dmab:Zol: 280 men, 625 women). Mortality risk was measured using sex-specific pairwise multivariable Cox models. In the fracture cohort, compared with no treatment, Dmab was associated with 48% lower mortality in women (hazard ratio [HR] = 0.52, 95% confidence interval [CI] 0.36-0.72) but not in men. Oral BPs were associated with 44% lower mortality in both sexes (women HR = 0.56, 95% CI 0.42-0.77; men HR = 0.56, 95% CI 0.40-0.78). In the no-fracture cohort, compared with BPs, Dmab was associated with 1.5- to 2.5-fold higher mortality than oral BPs (women HR = 1.49, 95% CI 1.13-1.98; men HR = 2.74; 95% CI 1.82-4.11) but similar mortality to Zol. Dmab in women and oral BPs were associated with lower post-fracture mortality than no treatment. However, Dmab users had generally higher mortality than oral BP users in those without fractures. © 2023 American Society for Bone and Mineral Research (ASBMR).
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